AtlasHvem vi hjælperVores videnskabProdukterResultater
Log indSpørgSekvenér dit genom↗
Træk
Loss of bowel control
Klinisk navn: Bowel incontinence
Involuntary fecal soiling in adults and children who have usually already been toilet trained.
Resumé
- Også kaldet
- Anal incontinence, Faecal incontinence, Fecal incontinence
AtlasHvem vi hjælperVores videnskabProdukterResultater
Log indSpørgSekvenér dit genom↗
Denne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/bowel-incontinence.json"
page <- fromJSON(url)
page$trait$nameLoss of bowel controlHP:0002607
AtlasHvem vi hjælperVores videnskabProdukterResultater
Log indSpørgSekvenér dit genom↗
Læs de gener, der er knyttet til Loss of bowel control, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test44 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Metachromatic LeukodystrophyReads 2 of these genesARSAPSAPAbout this report →
- Hereditary Spastic ParaplegiaReads 9 of these genesABCD1DSTYKPLP1ATP13A2DDHD2FA2HAbout this report →
- 22q11.2 Deletion SyndromeReads 1 of these genesTBX1About this report →
- Christianson SyndromeReads 1 of these genesSLC9A6About this report →
Show 40 more reports
- FGFR3-Related Chondrodysplasias (Achondroplasia and Related Conditions)Reads 1 of these genesFGFR3About this report →
- Fragile X SyndromeReads 1 of these genesFMR1About this report →
- Mowat-Wilson SyndromeReads 1 of these genesZEB2About this report →
- SCN4A-Related Congenital MyopathyReads 1 of these genesSCN4AAbout this report →
- Townes-Brocks SyndromeReads 1 of these genesSALL1About this report →
- X-Linked Adrenoleukodystrophy (ABCD1)Reads 1 of these genesABCD1About this report →
- Inherited Neurodegenerative DisordersReads 17 of these genesABCD1DSTYKPLP1SLC44A1ARSAATP13A2About this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesHTRA1About this report →
- Congenital Disaccharidase DeficienciesReads 1 of these genesSIAbout this report →
- Familial Periodic ParalysisReads 1 of these genesSCN4AAbout this report →
- Other Inherited LeukodystrophiesReads 4 of these genesABCD1PLP1ARSAPSAPAbout this report →
- Inherited Platelet Function DisordersReads 1 of these genesGP1BBAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesATP13A2About this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 1 of these genesDSTYKAbout this report →
- Hermansky-Pudlak SyndromeReads 1 of these genesHPS6About this report →
- Frontotemporal DementiaReads 1 of these genesVCPAbout this report →
- Myofibrillar MyopathiesReads 1 of these genesKYAbout this report →
- Female InfertilityReads 2 of these genesFMR1TP63About this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesATP13A2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 4 of these genesARSAPSAPRTN2VCPAbout this report →
- Lysosomal Storage DiseaseReads 2 of these genesARSAPSAPAbout this report →
- Parkinson DiseaseReads 1 of these genesATP13A2About this report →
- Ectodermal DysplasiasReads 1 of these genesTP63About this report →
- Distal MyopathiesReads 1 of these genesVCPAbout this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesRTN2VCPAbout this report →
- Noonan SyndromeReads 1 of these genesMAPK1About this report →
- Syndromic CraniosynostosisReads 1 of these genesFGFR3About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPLP1About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesSCN4AAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesVCPAbout this report →
- Inherited ThrombocytopeniasReads 1 of these genesGP1BBAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesNOP56About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesSCN4AAbout this report →
- Male InfertilityReads 1 of these genesCFAP43About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesFLVCR1About this report →
- Intellectual DisabilityReads 2 of these genesZEB2JMJD1CAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesMAPK1About this report →
- Retinitis PigmentosaReads 1 of these genesFLVCR1About this report →
- Epilepsy (Full Panel)Reads 1 of these genesZEB2About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesTBX1About this report →
Læs de gener, der er knyttet til Loss of bowel control, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test47 gener knyttet til Loss of bowel control
Ændringer i disse gener forårsager sjældne tilstande, hvor Loss of bowel control ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| HTRA1HtrA serine peptidase 1 | Altid | I 1 tilstand |
| KYkyphoscoliosis peptidase | Altid | I 1 tilstand |
| FUZfuzzy planar cell polarity protein | Meget ofte (80–99 %) | I 1 tilstand |
| VANGL1VANGL planar cell polarity protein 1 | Meget ofte (80–99 %) | I 1 tilstand |
| ABCD1ATP binding cassette subfamily D member 1 | Ofte (30–79 %) | I 2 tilstande |
| DSTYKdual serine/threonine and tyrosine protein kinase | Ofte (30–79 %) | I 1 tilstand |
| PLP1proteolipid protein 1 | Ofte (30–79 %) | I 1 tilstand |
| SLC44A1solute carrier family 44 member 1 | Ofte (30–79 %) | I 1 tilstand |
| ZEB2zinc finger E-box binding homeobox 2 | Ofte (30–79 %) | I 2 tilstande |
| ARSAarylsulfatase A | Nogle gange (5–29 %) | I 1 tilstand |
| ARVCFARVCF delta catenin family member | Nogle gange (5–29 %) | I 1 tilstand |
| ATP13A2ATPase cation transporting 13A2 | Nogle gange (5–29 %) | I 1 tilstand |
| BCRBCR activator of RhoGEF and GTPase | Nogle gange (5–29 %) | I 1 tilstand |
| COMTcatechol-O-methyltransferase | Nogle gange (5–29 %) | I 1 tilstand |
| CRKLCRK like proto-oncogene, adaptor protein | Nogle gange (5–29 %) | I 1 tilstand |
| DACT1dishevelled binding antagonist of beta catenin 1 | Nogle gange (5–29 %) | I 1 tilstand |
| DDHD2DDHD domain containing 2 | Nogle gange (5–29 %) | I 1 tilstand |
| EIF2AK2eukaryotic translation initiation factor 2 alpha kinase 2 | Nogle gange (5–29 %) | I 1 tilstand |
| FA2Hfatty acid 2-hydroxylase | Nogle gange (5–29 %) | I 1 tilstand |
| FGFR3fibroblast growth factor receptor 3 | Nogle gange (5–29 %) | I 1 tilstand |
| FMR1fragile X messenger ribonucleoprotein 1 | Nogle gange (5–29 %) | I 2 tilstande |
| GP1BBglycoprotein Ib platelet subunit beta | Nogle gange (5–29 %) | I 1 tilstand |
| HIRAhistone cell cycle regulator | Nogle gange (5–29 %) | I 1 tilstand |
| HPS6HPS6 biogenesis of lysosomal organelles complex 2 subunit 3 | Nogle gange (5–29 %) | I 1 tilstand |
| HPSE2heparanase 2 (inactive) | Nogle gange (5–29 %) | I 1 tilstand |
| ISL1ISL LIM homeobox 1 | Nogle gange (5–29 %) | I 1 tilstand |
| JMJD1Cjumonji domain containing 1C | Nogle gange (5–29 %) | I 1 tilstand |
| LRIG2leucine rich repeats and immunoglobulin like domains 2 | Nogle gange (5–29 %) | I 1 tilstand |
| MAPK1mitogen-activated protein kinase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| PSAPprosaposin | Nogle gange (5–29 %) | I 1 tilstand |
| RREB1ras responsive element binding protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RTN2reticulon 2 | Nogle gange (5–29 %) | I 1 tilstand |
| SALL1spalt like transcription factor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Nogle gange (5–29 %) | I 1 tilstand |
| SEC24CSEC24 homolog C, COPII component | Nogle gange (5–29 %) | I 1 tilstand |
| SIsucrase-isomaltase | Nogle gange (5–29 %) | I 1 tilstand |
| TBCDtubulin folding cofactor D | Nogle gange (5–29 %) | I 2 tilstande |
| TBX1T-box transcription factor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| TP63tumor protein p63 | Nogle gange (5–29 %) | I 1 tilstand |
| UBAP1ubiquitin associated protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
Vis 7 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| UFD1ubiquitin recognition factor in ER associated degradation 1 | Nogle gange (5–29 %) | I 1 tilstand |
| VCPvalosin containing protein | Nogle gange (5–29 %) | I 1 tilstand |
| FLVCR1FLVCR choline and heme transporter 1 | Sjældent (1–4%) | I 1 tilstand |
| NOP56NOP56 ribonucleoprotein | Sjældent (1–4%) | I 1 tilstand |
| CFAP43cilia and flagella associated protein 43 | Ikke registreret | I 1 tilstand |
| SLC9A6solute carrier family 9 member A6 | Ikke registreret | I 1 tilstand |
| ZFYVE26zinc finger FYVE-type containing 26 | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Snævrere træk
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.19-9814e911.
AtlasHvem vi hjælperVores videnskabProdukterResultater
Log indSpørgSekvenér dit genom↗
From traits to your genome
Read the genes behind these traits in your own DNA.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 810+ physician-ready reports.
Fra 449 $
Gratis forsendelse · Resultater på 6–8 uger
